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| | style="padding: 0 5px; font-size: 90%; background: #F5F5F5;" align=left | <sup>†</sup> Preferred in most patients greater than 65 y of age or patients with impairment of 8th cranial nerve function or renal function. <BR> <sup>‡</sup> Two-week regimen not intended for patients with known cardiac or extracardiac abscess or for those with creatinine clearance of less than 20 ml per min, impaired 8th cranial nerve function, or ''Abiotrophia'', ''Granulicatella'', or ''Gemella'' infection. <BR> <sup>¶</sup> Gentamicin dosage should be adjusted to achieve peak serum concentration of 3—4 μg/ml and trough serum concentration of less than 1 μg/ml when 3 divided doses are used; nomogram used for single daily dosing; other potentially nephrotoxic drugs (e.g., nonsteroidal anti-inflammatory drugs) should be used with caution in patients receiving gentamicin therapy. <BR> <sup>ǁ</sup> Vancomycin therapy recommended only for patients unable to tolerate penicillin or ceftriaxone; vancomycin dosage should be adjusted to obtain peak (1 h after infusion completed) serum concentration of 30–45 μg/ml and a trough concentration range of 10–15 μg/ml; vancomycin dosages should be infused during course of at least 1 h to reduce risk of histamine-release red man syndrome. | | | style="padding: 0 5px; font-size: 90%; background: #F5F5F5;" align=left | <sup>†</sup> Preferred in most patients greater than 65 y of age or patients with impairment of 8th cranial nerve function or renal function. <BR> <sup>‡</sup> Two-week regimen not intended for patients with known cardiac or extracardiac abscess or for those with creatinine clearance of less than 20 ml per min, impaired 8th cranial nerve function, or ''Abiotrophia'', ''Granulicatella'', or ''Gemella'' infection. <BR> <sup>¶</sup> Gentamicin dosage should be adjusted to achieve peak serum concentration of 3—4 μg/ml and trough serum concentration of less than 1 μg/ml when 3 divided doses are used; nomogram used for single daily dosing; other potentially nephrotoxic drugs (e.g., nonsteroidal anti-inflammatory drugs) should be used with caution in patients receiving gentamicin therapy. <BR> <sup>ǁ</sup> Vancomycin therapy recommended only for patients unable to tolerate penicillin or ceftriaxone; vancomycin dosage should be adjusted to obtain peak (1 h after infusion completed) serum concentration of 30–45 μg/ml and a trough concentration range of 10–15 μg/ml; vancomycin dosages should be infused during course of at least 1 h to reduce risk of histamine-release red man syndrome. |
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Revision as of 18:25, 5 March 2014
Pathogen-Based Therapy Adapted from Circulation 2008;118(15):e523-661.[1]
Viridans Streptococci or Streptococcus bovis
▸ Click on the following categories to expand treatment regimens.
Native Valve Endocarditis
▸ Penicillin-Susceptible, Adult
▸ Penicillin-Susceptible, Pediatric
▸ Penicillin-Resistant, Adult
▸ Penicillin-Resistant, Pediatric
Prosthetic Valve Endocarditis
▸ Penicillin-Susceptible, Adult
▸ Penicillin-Susceptible, Pediatric
▸ Penicillin-Resistant, Adult
▸ Penicillin-Resistant, Pediatric
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Adult
|
Preferred Regimen†
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 4 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 4 weeks
|
Alternative Regimen 1‡
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 2 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h x 2 weeks¶
|
Alternative Regimen 2
|
▸ Vancomycin 15 mg/kg IV q12h x 4 weeksǁ
|
† Preferred in most patients greater than 65 y of age or patients with impairment of 8th cranial nerve function or renal function. ‡ Two-week regimen not intended for patients with known cardiac or extracardiac abscess or for those with creatinine clearance of less than 20 ml per min, impaired 8th cranial nerve function, or Abiotrophia, Granulicatella, or Gemella infection. ¶ Gentamicin dosage should be adjusted to achieve peak serum concentration of 3—4 μg/ml and trough serum concentration of less than 1 μg/ml when 3 divided doses are used; nomogram used for single daily dosing; other potentially nephrotoxic drugs (e.g., nonsteroidal anti-inflammatory drugs) should be used with caution in patients receiving gentamicin therapy. ǁ Vancomycin therapy recommended only for patients unable to tolerate penicillin or ceftriaxone; vancomycin dosage should be adjusted to obtain peak (1 h after infusion completed) serum concentration of 30–45 μg/ml and a trough concentration range of 10–15 μg/ml; vancomycin dosages should be infused during course of at least 1 h to reduce risk of histamine-release red man syndrome.
|
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Pediatric
|
Preferred Regimen†
|
▸ Penicillin G sodium 0.2 MU/kg/day IV q4—6h x 4 weeks OR ▸ Ceftriaxone 100 mg/kg IV/IM q24h x 4 weeks
|
Alternative Regimen 1‡
|
▸ Penicillin G sodium 0.2 MU/kg/day IV q4—6h x 2 weeks OR ▸ Ceftriaxone 100 mg/kg IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h (or 1 mg/kg IV q8h) x 2 weeks¶
|
Alternative Regimen 2
|
▸ Vancomycin 40 mg/kg/day IV q8—12h x 4 weeksǁ
|
† Preferred in most patients greater than 65 y of age or patients with impairment of 8th cranial nerve function or renal function. ‡ Two-week regimen not intended for patients with known cardiac or extracardiac abscess or for those with creatinine clearance of less than 20 ml per min, impaired 8th cranial nerve function, or Abiotrophia, Granulicatella, or Gemella infection. ¶ Gentamicin dosage should be adjusted to achieve peak serum concentration of 3—4 μg/ml and trough serum concentration of less than 1 μg/ml when 3 divided doses are used; nomogram used for single daily dosing; other potentially nephrotoxic drugs (e.g., nonsteroidal anti-inflammatory drugs) should be used with caution in patients receiving gentamicin therapy. ǁ Vancomycin therapy recommended only for patients unable to tolerate penicillin or ceftriaxone; vancomycin dosage should be adjusted to obtain peak (1 h after infusion completed) serum concentration of 30–45 μg/ml and a trough concentration range of 10–15 μg/ml; vancomycin dosages should be infused during course of at least 1 h to reduce risk of histamine-release red man syndrome.
|
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Adult
|
Preferred Regimen
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 4 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 4 weeks
|
Alternative Regimen 1
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 2 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h x 2 weeks
|
Alternative Regimen 2
|
▸ Vancomycin 15 mg/kg IV q12h x 4 weeks
|
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Adult
|
Preferred Regimen
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 4 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 4 weeks
|
Alternative Regimen 1
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 2 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h x 2 weeks
|
Alternative Regimen 2
|
▸ Vancomycin 15 mg/kg IV q12h x 4 weeks
|
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Adult
|
Preferred Regimen
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 4 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 4 weeks
|
Alternative Regimen 1
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 2 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h x 2 weeks
|
Alternative Regimen 2
|
▸ Vancomycin 15 mg/kg IV q12h x 4 weeks
|
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Adult
|
Preferred Regimen
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 4 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 4 weeks
|
Alternative Regimen 1
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 2 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h x 2 weeks
|
Alternative Regimen 2
|
▸ Vancomycin 15 mg/kg IV q12h x 4 weeks
|
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Adult
|
Preferred Regimen
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 4 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 4 weeks
|
Alternative Regimen 1
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 2 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h x 2 weeks
|
Alternative Regimen 2
|
▸ Vancomycin 15 mg/kg IV q12h x 4 weeks
|
|
Viridans Streptococci or S. bovis NVE, PCN-Susceptible, Adult
|
Preferred Regimen
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 4 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 4 weeks
|
Alternative Regimen 1
|
▸ Penicillin G sodium 12—18 MU/day IV continuously/q4—6h x 2 weeks OR ▸ Ceftriaxone 2 g IV/IM q24h x 2 weeks
|
PLUS
|
▸ Gentamicin 3 mg/kg IV q24h x 2 weeks
|
Alternative Regimen 2
|
▸ Vancomycin 15 mg/kg IV q12h x 4 weeks
|
|
|
References
- ↑ Bonow, RO.; Carabello, BA.; Chatterjee, K.; de Leon, AC.; Faxon, DP.; Freed, MD.; Gaasch, WH.; Lytle, BW.; Nishimura, RA. (2008). "2008 focused update incorporated into the ACC/AHA 2006 guidelines for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to revise the 1998 guidelines for the management of patients with valvular heart disease). Endorsed by the Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, and Society of Thoracic Surgeons". J Am Coll Cardiol. 52 (13): e1–142. doi:10.1016/j.jacc.2008.05.007. PMID 18848134.